Updates on the latest developments in research, projects, fundraising and our community.
After being diagnosed with advanced leiomyosarcoma in 2024 and given just months to live, Gail Redpath from Edinburgh has defied expectations. Now living with incurable leiomyosarcoma, she shares…
For people living with rare cancers, the cost of travelling for treatment or staying away from home can add extra pressure at an already difficult time. The Sophie…
A diagnosis of Leiomyosarcoma can bring a wide range of emotions. Learn why what you're feeling is normal and where you can find support.
Find out how rare Leiomyosarcoma is, what "rare cancer" means and why specialist care and research are so important for people diagnosed with LMS.
Many people have never heard of Leiomyosarcoma until they are diagnosed. Learn why this rare cancer is less well known and why raising awareness is so important.
Wondering whether you should ask for a second opinion after a Leiomyosarcoma diagnosis? Learn when a second opinion may be helpful and what to expect.
Confused by the medical language used after a Leiomyosarcoma diagnosis? Our simple glossary explains some of the most common terms in plain English.
Wondering what an MDT meeting is after a Leiomyosarcoma diagnosis? Learn what happens, who attends and how multidisciplinary teams help plan your treatment.
Learn what a specialist sarcoma centre is, why you may be referred there after a Leiomyosarcoma diagnosis and how specialist teams help plan your care.
Learn how Leiomyosarcoma is diagnosed, the tests you may have and why specialist sarcoma teams play an important role in confirming a diagnosis.
Preparing for your first appointment after a Leiomyosarcoma diagnosis? Here are some helpful questions you may wish to ask your consultant and healthcare team.
A diagnosis of Leiomyosarcoma can feel overwhelming. Learn what usually happens next, who will be involved in your care and where to find trusted information and support.
